2-[(2,6-Dimethylphenoxy)methyl]oxirane

Base Information

• Chemical Name: 2-[(2,6-Dimethylphenoxy)methyl]oxirane
• CAS No.: 5296-34-4
• Molecular Formula: C11H14O2
• Molecular Weight: 178.231
• Hs Code.: 2910900090
• DSSTox Substance ID: DTXSID60395904
• Nikkaji Number: J1.061.545C
• Mol file: 5296-34-4.mol

Synonyms:2-[(2,6-dimethylphenoxy)methyl]oxirane;5296-34-4;2-((2,6-dimethylphenoxy)methyl)oxirane;SCHEMBL3671560;DTXSID60395904;(2,6-Dimethylphenyl)glycidyl ether;MFCD02171144;AKOS000200903;AKOS017278329;CS-0221743;EN300-09933;Z104492282

Chemical Property of 2-[(2,6-Dimethylphenoxy)methyl]oxirane

Chemical Property:

• Vapor Pressure: 0.0161mmHg at 25°C
• Boiling Point: 264.2°Cat760mmHg
• Flash Point: 102.7°C
• PSA: 21.76000
• Density: 1.071g/cm³
• LogP: 2.08100
• XLogP3: 2.3
• Hydrogen Bond Donor Count: 0
• Hydrogen Bond Acceptor Count: 2
• Rotatable Bond Count: 3
• Exact Mass: 178.099379685
• Heavy Atom Count: 13
• Complexity: 160

Purity/Quality:

99% ^*data from raw suppliers

2-[(2,6-dimethylphenoxy)methyl]oxirane ^*data from reagent suppliers

Safty Information:

• Pictogram(s):  
• Hazard Codes: 

MSDS Files:

SDS file from LookChem

Useful:

• Canonical SMILES: CC1=C(C(=CC=C1)C)OCC2CO2

Technology Process of 2-[(2,6-Dimethylphenoxy)methyl]oxirane

There total 5 articles about 2-[(2,6-Dimethylphenoxy)methyl]oxirane which guide to synthetic route it. The literature collected by LookChem mainly comes from the sharing of users and the free literature resources found by Internet computing technology. We keep the original model of the professional version of literature to make it easier and faster for users to retrieve and use. At the same time, we analyze and calculate the most feasible synthesis route with the highest yield for your reference as below:

synthetic route:

Reference yield: 80.0%

2.6-dimethylphenol (576-26-1,25134-01-4) + epichlorohydrin (106-89-8,24969-06-0,13403-37-7) → 2,6-dimethylphenyl glycidyl ether (5296-34-4)

Guidance literature:

With potassium carbonate; In acetone; for 20h; Reflux;

DOI:10.1016/j.tetasy.2009.11.014

Reference yield: 38.0%

→ 2,6-dimethylphenyl glycidyl ether (5296-34-4)

Guidance literature:

Reference yield:

1-chloro-3-(2,6-dimethyl-phenoxy)-propan-2-ol (103861-40-1) → 2,6-dimethylphenyl glycidyl ether (5296-34-4)

Guidance literature:

With sodium hydroxide; In tetrahydrofuran; at 20 - 60 ℃; for 0.666667h;

DOI:10.1021/jm00177a015

upstream raw materials:

2.6-dimethylphenol

epichlorohydrin

1-chloro-3-(2,6-dimethyl-phenoxy)-propan-2-ol

Downstream raw materials:

1-(2,6-dimethyl-phenoxy)-3-piperidin-1-yl-propan-2-ol

dl-1-(2,6-Dimethylphenoxy)-2-hydroxy-3-dimethylaminopropane

GD-8

dl-N-<3-(2,6-Dimethylphenoxy)-2-hydroxypropyl>-N-(4-bromophenacyl)-N,N-dimethylammonium bromide

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